Canonical Allele Identifier: CA2573144666

Gene:

Linked Data

• ClinVar Variation Id: 1522450
• ClinVar RCV Id: RCV002034433
• dbSNP Id: rs536842279
• gnomAD v4: 9-35658092-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658092G>A , CM000671.2:g.35658092G>A	GRCh38
NC_000009.11:g.35658089G>A , CM000671.1:g.35658089G>A	GRCh37
NC_000009.10:g.35648089G>A	NCBI36
NG_017041.1:g.4927C>T , LRG_163:g.4927C>T
NG_033120.1:g.4803G>A